Preferred Label : Laurin-Sandrow syndrome;
ICD-11 definition : Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete
polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal
alae and short columella), often associated with ulnar and/or fibular duplication
(and sometimes tibial agenesis).;
Origin ID : 671594481;
Automatic exact mappings (from CISMeF team)
Laurin-Sandrow syndrome is a developmental anomalies syndrome characterised by complete
polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal
alae and short columella), often associated with ulnar and/or fibular duplication
(and sometimes tibial agenesis).
